US4026895A - 1,3-Benzodioxol derivatives - Google Patents
1,3-Benzodioxol derivatives Download PDFInfo
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- US4026895A US4026895A US05/609,145 US60914575A US4026895A US 4026895 A US4026895 A US 4026895A US 60914575 A US60914575 A US 60914575A US 4026895 A US4026895 A US 4026895A
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- benzodioxol
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
Definitions
- This invention relates to 1,3-benzodioxol derivatives, the new compounds. More particularly, the invention relates to 1,3-benzodioxol derivatives represented by the following formula: ##STR2## wherein R 1 and R 2 are lower alkyls or the both together in interconnection may form a divalent alkylene as a member constituting a cyclic structural moiety; R 3 is a lower alkyl, phenyl, halogen-substituted phenyl or benzhydryl group, n is an integer of 2 or 3, and X stands for carbonyl (CO) or methylene (CH 2 ) bridge, and a process for the synthesis thereof.
- R 1 and R 2 are lower alkyls or the both together in interconnection may form a divalent alkylene as a member constituting a cyclic structural moiety
- R 3 is a lower alkyl, phenyl, halogen-substituted phenyl or benzhydry
- 1,3-Benzodioxol derivatives of the formula (I) wherein X stands for the carbonyl may be prepared, for example, by the following schematic equation: ##STR3## wherein R 1 , R 2 , R 3 and n have the meanings same as those defined with respect to the formula (I) aforementioned.
- the amide compound of the formula (IV) is obtained by subjecting 2,2-di-lower-alkyl-substituted 1,3-benzodioxol-5-carboxylic acid of the formula (II) or a reactive derivative thereof to reaction with 1-substituted 1,4-diazacycloalkane of the formula (III).
- Preferable class of the reactive derivatives of the starting carboxylic acid compound of the formula (II) is the corresponding acid anhydride, mixed acid anhydride, acid halide, and reactive ester thereof.
- the reaction can advantageously be effected in the presence of an organic solvent inert to the reaction system, such as benzene, toluene, xylene, acetone, pyridine and the like.
- the contemplated reaction can be performed smoothly by the addition of an acid-binding agent, such as pyridine, triethylamine, alkali carbonate, caustic alkali and the like, to the reaction system, when the acid halide, such as acid chloride, of the carboxylic acid derivative of the formula (II) is employed.
- Pyridine will serve both as the acid-binding agent and also the solvent in the system.
- 1,3-benzodioxol derivatives of the aforementioned formula (I) wherein X stands for the methylene may be obtained by the reduction of the compound of the formula (IV) in accordance with the following chemical equation: ##STR4## wherein R 1 , R 2 , R 3 and n have the meanings same as those defined in the preceding formulae.
- a metal complex compounds such as lithiumaluminium hydride, sodium dihydro-bis(2-methoxy, ethoxy)aluminate and the like, and the method where a high pressure and high temperature gaseous hydrogen is employed in the presence of cupper-nickel catalyst.
- solvent for recrystallization of the resulting reduction product there may be employed with good result any of lower alcohols, such as methanol, ethanol, propanol and a mixture of any of said alcohols with ethyl ether.
- lower alcohols such as methanol, ethanol, propanol and a mixture of any of said alcohols with ethyl ether.
- the resultant compounds (I), if desired, may be converted into the pharmacologically acceptable acid-addition salts thereof in accordance with a conventional salt-forming procedure.
- pharmacologically acceptable acids preferable for the formation of the acid-addition salts, there may be mentioned inorganic acids such as hydrochloric, sulfuric, nitric and the like acids; and organic acids such as acetic, citric, tartaric, oxalic, fumaric, maleic, methane-sulfonic and the like acids.
- Anti-histamic activity presented by the compounds of the present invention was measured on the isolated organs obtained by extirpation from guinea-pig or rat by means of Magnus apparatus as follows:
- the new compounds of the present invention exhibit the marked anti-histamic, anti-serotonine, anti-choline and the like activities characterized their good durability, and accordingly, they are highly useful as anti-histamic agent for therapeutic treatments.
- the esteral extract is washed with water, dried on magnesium sulfate, and the solvent is distilled off from the dry extract. There are obtained 4.5 grams of the residue.
- the resulting product is in afree base which is identified by converting it into the corresponding hydrochloride as follows:
- 2,2-Dimethyl-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-methyl-piperazine in accordance with the procedure disclosed in Example 1.
- the purposed reaction product is identified as its hydrochloride having a melting point of 230°-240° C.
- Elementary analysis of the hydrochloride of the product having presumable formula C 15 H 20 N 2 O 3 .sup.. HCl.sup.. 1/4H 2 O gives the following data:
- 2,2-Dimethyl-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-methyl-homopiperazine in accordance with the procedure disclosed inExample 1.
- the contemplated reaction product thus obtained is identified ina form of its hydrochloride having a melting point of 190°-198° C.
- Elementary analysis of the hydrochloride havingthe presumable formula C 16 H 22 N 2 O 3 .sup. . HCl.sup.. 1/2H 2 O gives the following data:
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Abstract
1,3-Benzodioxol derivatives, the new compounds, represented by the formula: ##STR1## and the pharmacologically acceptable acid-addition salts thereof are provided, wherein R1 and R2 are lower alkyls or the both together may form a divalent alkylene, R3 is a lower alkyl, phenyl, halogen-substituted phenyl or benzhydryl group, n is an integer of 2 or 3, and X stands for carbonyl (CO) or methylene (CH2) bridge. The compounds in which X stands for the methylene exhibit durable anti-histamic activity with low toxicity, and are useful for therapeutic purposes, while the compounds in which X stands for the carbonyl bridge are easily convertible by reduction into the former compounds.
Description
This is a division of application Ser. No. 503,515, filed Sept. 5, 1974, now U.S. Pat. No. 3,981,864 issued Sept. 21, 1976.
This invention relates to 1,3-benzodioxol derivatives, the new compounds. More particularly, the invention relates to 1,3-benzodioxol derivatives represented by the following formula: ##STR2## wherein R1 and R2 are lower alkyls or the both together in interconnection may form a divalent alkylene as a member constituting a cyclic structural moiety; R3 is a lower alkyl, phenyl, halogen-substituted phenyl or benzhydryl group, n is an integer of 2 or 3, and X stands for carbonyl (CO) or methylene (CH2) bridge, and a process for the synthesis thereof.
It has been found that the new compounds of this invention possess anti-histamic activity and in particular 1,3-benzodioxol derivatives of the abovementioned formula (I) wherein X stands for the methylene bridge possess durable anti-histamic activity with low toxicity.
1,3-Benzodioxol derivatives of the formula (I) wherein X stands for the carbonyl may be prepared, for example, by the following schematic equation: ##STR3## wherein R1, R2, R3 and n have the meanings same as those defined with respect to the formula (I) aforementioned. Thus, the amide compound of the formula (IV) is obtained by subjecting 2,2-di-lower-alkyl-substituted 1,3-benzodioxol-5-carboxylic acid of the formula (II) or a reactive derivative thereof to reaction with 1-substituted 1,4-diazacycloalkane of the formula (III).
Preferable class of the reactive derivatives of the starting carboxylic acid compound of the formula (II) is the corresponding acid anhydride, mixed acid anhydride, acid halide, and reactive ester thereof. The reaction can advantageously be effected in the presence of an organic solvent inert to the reaction system, such as benzene, toluene, xylene, acetone, pyridine and the like. The contemplated reaction can be performed smoothly by the addition of an acid-binding agent, such as pyridine, triethylamine, alkali carbonate, caustic alkali and the like, to the reaction system, when the acid halide, such as acid chloride, of the carboxylic acid derivative of the formula (II) is employed. Pyridine will serve both as the acid-binding agent and also the solvent in the system.
On the other hand, 1,3-benzodioxol derivatives of the aforementioned formula (I) wherein X stands for the methylene may be obtained by the reduction of the compound of the formula (IV) in accordance with the following chemical equation: ##STR4## wherein R1, R2, R3 and n have the meanings same as those defined in the preceding formulae.
In carrying out the reduction procedure, there may be employed, for example, the method wherein a metal complex compounds such as lithiumaluminium hydride, sodium dihydro-bis(2-methoxy, ethoxy)aluminate and the like, and the method where a high pressure and high temperature gaseous hydrogen is employed in the presence of cupper-nickel catalyst.
As solvent for recrystallization of the resulting reduction product, there may be employed with good result any of lower alcohols, such as methanol, ethanol, propanol and a mixture of any of said alcohols with ethyl ether.
The resultant compounds (I), if desired, may be converted into the pharmacologically acceptable acid-addition salts thereof in accordance with a conventional salt-forming procedure. As the pharmacologically acceptable acids preferable for the formation of the acid-addition salts, there may be mentioned inorganic acids such as hydrochloric, sulfuric, nitric and the like acids; and organic acids such as acetic, citric, tartaric, oxalic, fumaric, maleic, methane-sulfonic and the like acids.
Anti-histamic activity presented by the compounds of the present invention was measured on the isolated organs obtained by extirpation from guinea-pig or rat by means of Magnus apparatus as follows:
With 2-methyl-2-ethyl-5-(N-benzhydryl-piperazino-N'-methylene)-1,3-benzodioxol, the product of Example 9 hereinafter mentioned.
Contraction of the isolated ileum under external tension caused by one gram load to be produced by applying 10- 7 g/ml of histamine was retardatively controlled to an extent of 1/4 of the expected normal contraction, when the ileum has previously been treated with 10- 5 g/ml of said compound. It has further been found that said retardative behavior did not disappear when the treated ileum was rinsed with Tyrode's solution more than 5 times in the interval of 3 minutes. The fact apparently substantiates that the compound possesses durable anti-histamic activity.
With 5'-(N-methyl-homopiperazino-N' -methylene)-spirocyclohexano-1',3'-benzodioxol, the product of Example 15 hereinafter-mentioned, the following several MEC (Minimum Effective Concentrations) have been observed.
______________________________________
MEO
Anti-histamic activity: 10.sup.-.sup.5 g/ml
Anti-serotonine activity:
10.sup.-.sup.5 g/ml
Control: Cyproheptamine 2 × 10.sup.-.sup.6 g/ml
Anti-cholinergic activity:
10.sup.-.sup.5 g/ml
Uterine relaxatin activity:
10.sup.-.sup.5 g/ml
Control: Isoxsuprine 10.sup.-.sup.5 g/ml
Intestinal organ relaxation activity:
10.sup.-.sup.5 g/ml
Control: Papaverine 10.sup.-.sup.6 g/ml
______________________________________
Toxicity in I.P.A. (Intraperitoneal administration):
No appreciable toxic symptom appeared with 100 mg/kg.
As is evident from the above observations, the new compounds of the present invention exhibit the marked anti-histamic, anti-serotonine, anti-choline and the like activities characterized their good durability, and accordingly, they are highly useful as anti-histamic agent for therapeutic treatments.
The following Examples serve to illustrate the invention but they are, of course, not intended to limit it thereto.
3 Grams of 2-methyl-2-ethyl-1,3-benzodioxol-5-carboxylic acid are dissolvedin 4 ml of pyridine. To the resulting solution under ice-cooling with stirring, there are added 1.5 grams of thionyl chloride. After continuing the stirring for further 10 minutes, there are added 3.7 grams of N-benzhydryl-piperazine, and the mixture is heated on water bath for 30 minutes. Ice-water is added to the reaction mixture, and the acidic solution is made alkaline by neutralizing with a 5% aqueous sodium hydroxide solution. Oily substance separated out is extracted with ethyl acetate ester. The esteral extract is washed with water, dried on magnesium sulfate, and the solvent is distilled off from the dry extract. There are obtained 4.5 grams of the residue. The resulting product is in afree base which is identified by converting it into the corresponding hydrochloride as follows:
To a quotient of the residue, there are added a 10% ethanolic hydrochloric acid. The solution thus obtained is concentrated under reduced pressure todryness. The residue is crystallized from ethanol and has a melting point of 200°-210° C. Elementary analysis of the hydrochloride having the presumable formula C28 H30 N2 O3.sup.. HCl gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
69.34 6.58 5.78
Found (%):
69.37 6.57 5.72
______________________________________
In accordance with the procedure given in the preceding Example, 2-methyl-2-ethyl-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-methyl-homopiperazine. The product thus obtained is identified as its hydrochloride having a melting point of 218°-220° C. Elementary analysis of the hydrochloride havingthe presumable formula C17 H24 N2 O3.sup.. HCl gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
59.90 7.39 8.21
Found (%):
59.70 7.51 8.20
______________________________________
2-cyclohexyl-spiro-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-methyl-piperazine in accordance with the procedure given in Example 1. The reaction product thus obtained is identified as its hydrochloride having a melting point of 260°-270° C. Elementary analysis of the hydrochloride of the product having the presumable formula C18 H24 N2 O3.sup.. HCl gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
61.27 7.14 7.93
Found (%):
61.24 7.22 8.03
______________________________________
2-Cyclohexyl-spiro-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-benzhydryl-piperazine, in accordance with the procedure given in Example 1. The purposed reaction product thus obtained is identified as its hydrochloride having a melting point of 218°-222° C. Elementary analysis of the hydrochloride of theproduct having the presumable formula C30 H32 N2 O3.sup.. HCl gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
71.34 6.58 5.54
Found (%):
71.67 6.62 5.53
______________________________________
2,2-Dimethyl-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-methyl-piperazine in accordance with the procedure disclosed in Example 1. The purposed reaction product is identified as its hydrochloride having a melting point of 230°-240° C. Elementary analysis of the hydrochloride of the product having presumable formula C15 H20 N2 O3.sup.. HCl.sup.. 1/4H2 O gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
56.78 6.83 8.82
Found (%):
57.07 6.85 8.86
______________________________________
2,2-Dimethyl-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-methyl-homopiperazine in accordance with the procedure disclosed inExample 1. The contemplated reaction product thus obtained is identified ina form of its hydrochloride having a melting point of 190°-198° C. Elementary analysis of the hydrochloride havingthe presumable formula C16 H22 N2 O3.sup. . HCl.sup.. 1/2H2 O gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
57.21 7.20 8.34
Found (%):
57.32 7.27 7.30
______________________________________
2-Methyl-2-ethyl-1,3-benzodioxol-5-carboxylic acid is subjected to reactionwith N-methyl-piperazine in accordance with the procedure disclosed in Example 1. The resulting reaction product is identified in a form of its hydrochloride having a melting point of 190°-200° C. Elementary analysis of the hydrochloride having the presumable formula C16 H22 N2 O3.sup.. HCl.sup.. 3/4H2 O gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
56.72 7.28 8.26
Found (%):
59.32 7.29 7.30
______________________________________
2-Cyclohexyl-spiro-1,3-benzodioxol-5-carboxylic acid is subjected to reaction with N-methyl-homopiperazine in accordance with the procedure disclosed in Example 1. The contemplated reaction product thus obtained isidentified in a form of its hydrochloride having a melting point of 233°-237° C. Elementary analysis of the hydrochloride havingthe presumable formula C19 H26 N2 O3.sup.. HCl gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
62.20 7.41 7.63
Found (%):
62.04 7.48 7.82
______________________________________
4.0 Grams of 2-methyl-2-ethyl-5-(N-benzhydryl-piperazino)-N'-carbonyl-1,3-benzodioxol are introduced into a benzene solution containing 3 grams of sodium dihydro-bis(2-methoxy, ethoxy)aluminate. The mixture is warmed at 80° C. with stirring for two hours.
To the liquid reaction mixture under ice-cooling, there is added water, andthe mixture is extracted with ether. The etheral extract is washed with water, dried on magnesium sulfate, and the solvent is removed by distillation under reduced pressure. A 10% ethanolic hydrochloric acid is added to the residue and the mixture is concentrated under reduced pressure to dryness. The residue is recrystallized from a mixture of ethanol and ethyl ether to obtain the hydrochloride of the purposed product with 4.1 grams of yield, and having a melting point of 219°-221° C.
Elementary analysis of the hydrochloride having the presumable formula C28 H32 N2 O2.sup.. 2HCl.sup. . 1/3 H2 O gives the following data:
______________________________________
C H N
______________________________________
Calculated (%):
67.05 6.83 5.59
Found (%):
67.02 6.88 5.57
______________________________________
Further working Examples 10-21 are conducted in accordance with the procedure analoguous to that disclosed in the preceding Example 9. The data of the products thus obtained are listed in the following Table.
TABLE 1
__________________________________________________________________________
##STR5##
__________________________________________________________________________
No. of Example
R.sub.1
R.sub.2
R.sub.3 n
##STR6##
##STR7##
__________________________________________________________________________
10 CH.sub.3
C.sub.2 H.sub.5
CH.sub.3 3
##STR8##
##STR9##
##STR10##
##STR11##
11 (CH.sub.2).sub.5
CH.sub.3 2
##STR12##
##STR13##
##STR14##
##STR15##
12 (CH.sub.2).sub.5
2##STR16##
##STR17##
##STR18##
##STR19##
##STR20##
13 CH.sub.3
CH.sub.3
CH.sub.3 2
##STR21##
##STR22##
##STR23##
##STR24##
14 CH.sub.3
C.sub.2 H.sub.5
CH.sub.3 2
##STR25##
##STR26##
##STR27##
##STR28##
15 (CH.sub.2).sub.5
CH.sub.3 3
##STR29##
##STR30##
##STR31##
##STR32##
16 CH.sub.3
CH.sub.3
##STR33##
2
##STR34##
##STR35##
##STR36##
##STR37##
17 CH.sub.3
C.sub.2 H.sub.5
2##STR38##
##STR39##
##STR40##
##STR41##
##STR42##
18 (CH.sub.2).sub.4
CH.sub.3 2
##STR43##
##STR44##
##STR45##
##STR46##
19 (CH.sub.2).sub.4
2##STR47##
##STR48##
##STR49##
##STR50##
20 (CH.sub.2).sub.4##STR51##
2##STR52##
##STR53##
##STR54##
##STR55##
21 (CH.sub.2).sub.4##STR56##
2##STR57##
##STR58##
##STR59##
##STR60##
##STR61##
__________________________________________________________________________
Claims (6)
1. A member of the group consisting of a compound of the formula: ##STR62## wherein R1 and R2 are respectively lower alkyl of 1 to 2 carbon atoms or both R1 and R2 together form divalent alkylene of 5 carbon atoms as a part of a cyclic structural moiety; and R3 is methyl, phenyl, chlorophenyl or benzhydryl; and a pharmacologically acceptable acid-addition salt thereof.
2. A compound according to claim 1 wherein R1 is --Ch3, R2 is --C2 H5 and R3 is benzhydryl.
3. A compound according to claim 1 wherein R1 is --CH3, R2 is --C2 H5 and R3 is --CH3.
4. A compound according to claim 1 wherein R1 and R2 together represent the group --(CH2)5 -- and R3 represents --CH3.
5. A compound according to claim 1 wherein R1 and R2 together represent --(CH2)5 -- and R3 represents benzhydryl.
6. A compound according to claim 1 wherein R1, R2 and R3 represent --CH3.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/609,145 US4026895A (en) | 1973-09-08 | 1975-08-29 | 1,3-Benzodioxol derivatives |
| US05/684,735 US4051125A (en) | 1973-09-08 | 1976-05-10 | 1,3-Benzodioxol derivatives |
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JA48-100762 | 1973-09-08 | ||
| JP10076273A JPS5835194B2 (en) | 1973-09-08 | 1973-09-08 | 1,3- Benzoxole |
| JA48-100761 | 1973-09-08 | ||
| JP10076173A JPS596877B2 (en) | 1973-09-08 | 1973-09-08 | 1,3-benzodioxole |
| US05/503,515 US3981864A (en) | 1973-09-08 | 1974-09-05 | 1,3-Benzodioxol derivatives |
| US05/609,145 US4026895A (en) | 1973-09-08 | 1975-08-29 | 1,3-Benzodioxol derivatives |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/503,515 Division US3981864A (en) | 1973-09-08 | 1974-09-05 | 1,3-Benzodioxol derivatives |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/684,735 Division US4051125A (en) | 1973-09-08 | 1976-05-10 | 1,3-Benzodioxol derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4026895A true US4026895A (en) | 1977-05-31 |
Family
ID=27468859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/609,145 Expired - Lifetime US4026895A (en) | 1973-09-08 | 1975-08-29 | 1,3-Benzodioxol derivatives |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US4026895A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4734416A (en) * | 1978-03-30 | 1988-03-29 | Otsuka Pharmaceutical Co., Ltd. | Pharmaceutically useful carbostyril derivatives |
| US20070161791A1 (en) * | 2006-01-09 | 2007-07-12 | Narsimha Reddy Penthala | Process for the preparation of terazosin hydrocloride dihydrate |
| US20080027136A1 (en) * | 1998-02-11 | 2008-01-31 | Faller Douglas V | Compositions and methods for the treatment of cystic fibrosis |
| US20090082444A1 (en) * | 1993-03-31 | 2009-03-26 | The Trustees Of Boston University | Compositions for the Treatment of Blood Disorders |
| US20110033946A1 (en) * | 2009-03-11 | 2011-02-10 | Hemaquest Pharmaceuticals, Inc. | Detection of short-chain fatty acids in biological samples |
| US10857152B2 (en) | 2010-03-11 | 2020-12-08 | Trustees Of Boston University | Methods and compositions for treating viral or virally-induced conditions |
| US10953011B2 (en) | 2019-05-31 | 2021-03-23 | Viracta Therapeutics Inc. | Methods of treating virally associated cancers with histone deacetylase inhibitors |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3119826A (en) * | 1961-04-12 | 1964-01-28 | Snc Science Union Et Compagnie | Piperazine derivatives |
| US3981864A (en) * | 1973-09-08 | 1976-09-21 | Eisai Co., Ltd. | 1,3-Benzodioxol derivatives |
-
1975
- 1975-08-29 US US05/609,145 patent/US4026895A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3119826A (en) * | 1961-04-12 | 1964-01-28 | Snc Science Union Et Compagnie | Piperazine derivatives |
| US3981864A (en) * | 1973-09-08 | 1976-09-21 | Eisai Co., Ltd. | 1,3-Benzodioxol derivatives |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4734416A (en) * | 1978-03-30 | 1988-03-29 | Otsuka Pharmaceutical Co., Ltd. | Pharmaceutically useful carbostyril derivatives |
| US4824840A (en) * | 1978-03-30 | 1989-04-25 | Otsuka Pharmaceutical Co., Ltd. | Carbostyril derivatives and pharmaceutical preparations containing same |
| US20090082444A1 (en) * | 1993-03-31 | 2009-03-26 | The Trustees Of Boston University | Compositions for the Treatment of Blood Disorders |
| US20080027136A1 (en) * | 1998-02-11 | 2008-01-31 | Faller Douglas V | Compositions and methods for the treatment of cystic fibrosis |
| US20070161791A1 (en) * | 2006-01-09 | 2007-07-12 | Narsimha Reddy Penthala | Process for the preparation of terazosin hydrocloride dihydrate |
| US20110033946A1 (en) * | 2009-03-11 | 2011-02-10 | Hemaquest Pharmaceuticals, Inc. | Detection of short-chain fatty acids in biological samples |
| US10857152B2 (en) | 2010-03-11 | 2020-12-08 | Trustees Of Boston University | Methods and compositions for treating viral or virally-induced conditions |
| US12083119B2 (en) | 2010-03-11 | 2024-09-10 | Viracta Subsidiary, Inc. | Methods and compositions for treating viral or virally-induced conditions |
| US10953011B2 (en) | 2019-05-31 | 2021-03-23 | Viracta Therapeutics Inc. | Methods of treating virally associated cancers with histone deacetylase inhibitors |
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